Variant #0000301210 (NC_000017.10:g.66519972T>C, NM_017565.3:c.*13646A>G (FAM20A))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.66519972T>C
DNA change (hg38) g.68523831T>C
Published as PRKAR1A(NM_212471.2):c.440+15T>C
ISCN -
DB-ID PRKAR1A_000027
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00123 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARSG NM_001267727.1 -/. - c.*103368T>C r.(=) p.(=)
PRKAR1A NM_002734.4 -/. - c.440+15T>C r.(=) p.(=)
ARSG NM_014960.4 -/. - c.*103368T>C r.(=) p.(=)
FAM20A NM_017565.3 -/. - c.*13646A>G r.(=) p.(=)
WIPI1 NM_017983.5 -/. - c.-66410A>G r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.